U.S. flag

An official website of the United States government

Format
Items per page

Send to:

Choose Destination

Search results

Items: 1 to 20 of 171

    loading data ...

    Number of Variants: 20

    Variant Region IDTypeNumber of Variant CallsStudy IDOrganismClinical AssertionLocationGenes in region
    nsv3886923copy number variation1nstd102humanBenign GRCh37 chrX: 85,674,945-85,676,945 , GRCh38.p12 chrX: 86,419,942-86,421,942 DACH2
    nsv3874937copy number variation1nstd102humanBenign GRCh37 chrX: 85,797,122-85,932,574 , GRCh38.p12 chrX: 86,542,119-86,677,571 DACH2
    nsv3885282copy number variation1nstd102humanBenign GRCh37 chrX: 85,871,362-85,944,590 , GRCh38.p12 chrX: 86,616,359-86,689,587 DACH2
    nsv3883795copy number variation1nstd102humanLikely benign GRCh37 chrX: 85,588,096-86,011,611 , GRCh38.p12 chrX: 86,333,093-86,756,608 DACH2, FCF1P9
    nsv3887629copy number variation1nstd102humanBenign GRCh37 chrX: 85,871,362-86,456,938 , GRCh38.p12 chrX: 86,616,359-87,201,935 DACH2, COPS8P1
    nsv3888774copy number variation1nstd102humanBenign GRCh37 chrX: 86,044,208-86,224,601 , GRCh38.p12 chrX: 86,789,205-86,969,598 DACH2, COPS8P1
    nsv6636351copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,478,159-85,630,999 , GRCh38.p12 chrX: 86,223,156-86,375,996 DACH2, GEMIN8P3
    nsv4681813copy number variation1nstd102humanPathogenic GRCh37 chrX: 85,236,741-85,404,112 , GRCh38.p12 chrX: 85,981,737-86,149,108 DACH2, TPMTP4, 3 more genes
    nsv4451175copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,630,983-86,642,342 , GRCh38.p12 chrX: 86,375,980-87,387,339 DACH2, FCF1P9, 1 more genes
    nsv4452638copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,632,464-86,639,781 , GRCh38.p12 chrX: 86,377,461-87,384,778 DACH2, FCF1P9, 1 more genes
    nsv4728702copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,631,053-86,633,326 , GRCh38.p12 chrX: 86,376,050-87,378,323 DACH2, FCF1P9, 1 more genes
    nsv3876294copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,632,742-86,633,326 , GRCh38.p12 chrX: 86,377,739-87,378,323 DACH2, COPS8P1, 1 more genes
    nsv4683900copy number variation1nstd102humanUncertain significance GRCh37 chrX: 85,211,158-85,404,112 , GRCh38.p12 chrX: 85,956,153-86,149,108 DACH2, NDUFA5P7, 3 more genes
    nsv6314218complex chromosomal rearrangement7nstd102humanUncertain significance GRCh38.p12 chr8: 43,363,723-43,363,723 , GRCh38.p12 chr8: 43,363,730-43,363,730 , GRCh37 chr8: 43,218,866-43,218,866 , GRCh37 chr8: 43,218,873-43,218,873 , GRCh37 chrX: 86,011,605-86,011,605 , GRCh37 chrX: 86,011,605-86,011,605 , GRCh37 chrX: 87,270,917-87,270,917 , GRCh37 chrX: 87,270,918-87,270,918 , GRCh37 chrX: 111,784,479-111,784,479 , GRCh37 chrX: 111,784,525-111,784,525 , GRCh37 chrX: 152,943,075-152,943,075 , GRCh37 chrX: 152,943,335-152,943,335 , GRCh38.p12 chrX: 86,756,602-86,756,602 , GRCh38.p12 chrX: 86,756,602-86,756,602 , GRCh38.p12 chrX: 88,015,917-88,015,917 , GRCh38.p12 chrX: 88,015,918-88,015,918 , GRCh38.p12 chrX: 112,541,251-112,541,251 , GRCh38.p12 chrX: 112,541,297-112,541,297 , GRCh38.p12 chrX: 153,677,620-153,677,620 , GRCh38.p12 chrX: 153,677,880-153,677,880 , GRCh38.p12 chr2: 119,076,292-119,076,292 , GRCh38.p12 chr2: 119,076,293-119,076,293 , GRCh38.p12 chr2: 119,145,334-119,145,334 , GRCh38.p12 chr2: 119,145,359-119,145,359 , GRCh37 chr2: 119,833,868-119,833,868 , GRCh37 chr2: 119,833,869-119,833,869 , GRCh37 chr2: 119,902,910-119,902,910 , GRCh37 chr2: 119,902,935-119,902,935 DACH2, PNCK, 1 more genes
    nsv4682132copy number variation1nstd102humanPathogenic GRCh37 chrX: 84,634,178-85,404,112 , GRCh38.p12 chrX: 85,379,173-86,149,108 DACH2, CHM, 7 more genes
    nsv3904162copy number variation1nstd102humanPathogenic GRCh38 chrX: 10,001-156,030,895 , GRCh37 chrX: 60,001-155,260,560 , NCBI36 chrX: 1-154,913,754 DACH2, NANOGNBP3, 2154 more genes
    nsv3913255copy number variation2nstd102humanPathogenic NCBI36 chrX: 701-154,913,754 , GRCh37.p13 chrX: 60,701-155,260,560 , GRCh38.p12 chrX: 10,701-156,030,895 DACH2, NHS-AS1, 2154 more genes
    nsv3907094copy number variation4nstd102humanPathogenic GRCh38 chrX: 10,679-156,022,206 , GRCh37 chrX: 60,679-155,251,871 , NCBI36 chrX: 679-154,905,065 DACH2, GPR119, 2153 more genes
    nsv3878553copy number variation2nstd102humanPathogenic GRCh37 chrX: 60,262-155,245,765 , GRCh38.p12 chrX: 10,262-156,016,100 DACH2, H2AB2, 2152 more genes
    nsv3898149copy number variation1nstd102humanPathogenic GRCh38 chrX: 20,297-156,026,127 , NCBI36 chrX: 10,297-154,908,986 , GRCh37 chrX: 70,297-155,255,792 DACH2, OR3B1P, 2154 more genes
    Format
    Items per page

    Send to:

    Choose Destination

    Supplemental Content

    Filters: Manage Filters

    Find related data

    Search details

    See more...

    Recent activity

    Clear Turn Off Turn On

    Your browsing activity is empty.

    Activity recording is turned off.

    Turn recording back on

    See more...
    You are here: NCBI > Variation > Database of Genomic Structural Variation (dbVar)
    Support Center